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# FDA Seeks Comments on 510(k) Submission Requirements
- URL: https://www.fdaweb.com/fda-seeks-comments-on-510-k-submission-requirements/
- Published: 2016-11-18T12:00:00.000Z
- Updated: 2026-09-14T21:49:13.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5137380

*Federal Register* Notice: FDA is seeking comments on an information collection extension on medical device premarket notifications. The collection is related to Section 510(k) that requires a premarket notification submission to FDA at least 90 days before the introduction into interstate commerce of a device intended for human use. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2016-11-18/pdf/2016-27851.pdf?ref=fdaweb.com).